Cobetter, MINITFFS-HFEMI, Biophsep™ MiniLab TFF System, with FREE Hollow Fiber Module or TFF Cassette

Description
In the biopharmaceutical industry, researchers face challenges not only in the complexity of experiments, but also in how to process experimental data efficiently and accurately. To this end, Cobetter follows the core needs of biopharmaceutical developers and launches the easy-to-operate and comprehensive Biophsep™ TFF System - MiniLab experimental-grade ultrafiltration system.
This "R&D Helper" not only optimizes the experimental process, but also makes the operation easier and faster through its humanized design, greatly improving R&D efficiency. It can help researchers easily cope with various challenges in experiments and is suitable for process research or process characterization at different stages. From clarification to concentration to liquid exchange, every step is precise and efficient, ensuring the accuracy and reliability of experimental results.
Features
Small running volume and low testing cost; can be freely and flexibly matched
Produce key components on our own (PVC valves, single-use pressure sensors, balance)
Can be adapted to two types of consumables: hollow fiber membrane or membrane cassette
10 process modes
Manual/Automatic mode
Powerful function, can realize a variety of process operations
A variety of data can be collected and recorded
Suitable for basic process development at the R&D end
Applications
Constant TMP control
Constant ∆P control
NWP calculation
Continuous/discontinuous concentration
Shear rate calculation
Recipe management
Batch management/report management
Data processing/data export/trend analysis
Equal volume filtration
Simplified human-machine interaction
Based on Windows system operating software, it integrates powerful functions into a limited interface, including creating recipes, running experiments and viewing data. The core operations can be completed in three steps.
Compliance
Biophsep™ TFF System - MiniLab has complete user multi-level management permissions, complete audit tracking functions, and can meet regulatory requirements such as GMP and 21CFR Part 11.